Category Archives: Thorax

Can I Keep Patients With More Than Three Rib Fractures At My Level IV Trauma Center?

Rib fractures are one of the most common thoracic injuries presenting to trauma centers. Traditionally, many state designation standards set limits on the number of rib fractures in patients to be admitted to Level IV trauma centers. The assumption was that these centers had limited surgical capabilities and might not have the expertise to manage them to achieve optimal patient outcomes. They were then forced to transfer these patients upstream to a higher-level trauma center.

And then, unfortunately, COVID came along, and things changed. Mainly for the worse. Due to reduced professional staffing throughout the entire continuum of health care, the upstream centers are saturated and have limited availability to absorb patients who don’t take advantage of their increased resources.

Both staffing and reimbursement issues strain rural EMS agencies. It is difficult to justify transferring a patient to a center that takes the only ambulance in the community out of service for a good portion of the day. Also, most current state trauma system standards do not fully appreciate non-surgeon clinicians’ interest and skill levels at those Level IV centers.

The Pennsylvania Trauma Systems Foundation recognized these issues at the centers in its state. In 2020, it opted to liberalize the number of rib fractures that could be treated at Level IV centers. It required hospitalists to be current in ATLS in order to admit these patients. The centers were also required to adhere to a chest injury guideline created for them.

To gauge the safety and effectiveness of this change, a retrospective state registry study was performed comparing patients admitted during the 2.5 years before the standards change to the 2.5 years after. Demographics, injury characteristics, length of stay, and mortality were compared between the groups. Patients were excluded if they had significant injuries in other body regions, were age < 18 years of age, or had complicated fractures (requiring supplemental oxygen on admission, concomitant pneumothorax or hemothorax, pulmonary contusion or laceration, or who did not require admission

Here are the factoids:

  • Over 4,000 patients were recorded in the registry during the 5 years, but 3350 were excluded due to the definition of complex rib fractures
  • A final total of 1,070 patients were included, with 710 admitted to Level III centers and 360 to Level IV centers
  • This left 132 Level III patients and 228 Level IV patients in the pre- and post-standard groups, respectively
  • The number of transfers out of the Level IV centers dropped significantly, from 56% to 21%
  • Patients with <3 rib fractures had the same length of stay as those with more than three (3 vs 2, respectively)
  • Mortality was extremely low and not significantly different based on the number of rib fractures

Bottom line: This study showed that the change in admission standards for rib fractures in Pennsylvania did not impact outcomes and resulted in significantly fewer transfers.

The key to a successful change like this involves education and protocols. The requirement that hospitalists be current in ATLS is beneficial because it gives them a better understanding of the physiologic effects and priorities in managing trauma patients. A well-designed practice guideline is critical so that all clinicians apply best practices in caring for these patients. 

This is an important paper, and should be considered in any state where local resources are being challenged, and hospital reimbursements are declining. This type of standards change may breathe new life into many of our Level IV centers.

Chest Tube Size: The Argument That Never Dies

I’ve written many posts in the past about the arguments surrounding chest tube size: large bore vs. small bore (pigtail). For the longest time, only a few decent papers were looking into this debate, and subject numbers were small. The best the papers could say was that “small-bore chest tubes are not inferior to large-bore tubes.” Not that this is not the same as saying, “small-bore tubes are better than large-bore tubes.”

But finally, after more than ten years, there has been enough written on the topic that a pass at a systematic review and meta-analysis has been attempted.  The University of Miami Ryder Trauma Center group performed a comprehensive review of the topic, spanning literature published through 2022.

Here are the factoids:

  • A total of 2008 articles were identified, but after careful screening, only 11 articles met predetermined parameters for inclusion
  • There were 3 randomized, controlled studies, 3 prospective cohort studies, and 5 retrospective cohort studies
  • Two pairs of studies had overlapping patients, so only patients in the more recent study of each was included
  • The authors used CASP scoring to judge the quality and likelihood of bias. Nearly all studies included were of high quality.

And here are the interesting findings:

  • There was no significant difference in failure rates between small and large tubes (18% vs. 22% )
  • There were no differences in complication rates (12% vs. 13% )
  • There was a significantly higher amount of initial drainage with the small tubes (750 cc vs 400 cc) (??)
  • Although the overall number of complications was the same, there were significantly more insertion complications in the small-bore group (4.4 vs 2.2). These included intra-hepatic placement, malpositioned tubes, kinked tubes, and dislodgement.
  • Only one study used a validated pain score to measure insertion pain, and there was no difference between the tube sizes
  • Tube days averaged 1.5 days less in the small-bore group, which was significant. However, this did not impact ICU or hospital length of stay.

Bottom line: There are still significant limitations in this study due to the small number of randomized controlled trials that are yet available. I also worry that there is some selection bias in many of the studies that would cause large-bore tubes to be inserted preferentially into patients with more severe chest trauma, larger hemothorax, or more emergent need for the tube. However, if there were major, major differences, they would probably be starting to rear their heads by now.

The authors of this paper concluded that “small bore tube thoracostomy may be as effective as large bore thoracostomy for the management of patients with hemothorax.” They correctly suggest that guided studies examining which patients are more suited for a specific sized tube. I totally agree.

For now, I still don’t think there is a definitive answer. I recommend that the bedside trauma professional use their judgment regarding patient condition, the magnitude of the chest trauma, and the urgency of the procedure to select a size. They must also consider their expertise with the tube selected to maximize effectiveness and minimize complications.

I’m sure there will be even more to write on this topic. It doesn’t seem to want to die.

Reference:  Small versus large-bore thoracostomy for traumatic hemothorax: A systematic review and meta-analysis. Journal of Trauma and Acute Care Surgery 97(4):p 631-638, October 2024. | DOI: 10.1097/TA.0000000000004412

Prehospital: What’s The Best Chest Seal For Sucking Chest Wounds?

The treatment of a “sucking chest wound” in the field has typically been with application of some type of occlusive dressing. Many times, a generic adhesive dressing is applied, typically the same kind used to cover IV sites. This is quick, easy, cheap, and readily available in the ambulance. But there is a danger that this could result in development of tension pneumothorax, because the dressing not only keeps air from getting in but also keeps any buildup of pneumothorax from getting out.

To avoid this, a number of vented products have been developed and approved by the US Food and Drug Administration (FDA). These devices have some sort of system to allow drainage of accumulating air or blood, typically a one-way valve or drainage channels. They also need to stick well to a chest wall, which may have blood or other fluids that might disrupt the seal completely.

The US Army has a strong interest in making sure the products they use for this purpose work exactly as promised. The US Army Institute of Surgical Research examined 5 currently FDA-approved products to determine their ability to adhere to bleeding chest wounds, and to drain accumulating air and/or blood from the pleural space. They developed an open chest wound with active bleeding in a swine model.

An open hemopneumothorax was created by infusing air and blood, the animal was stabilized, then additional aliquots of air and blood were infused to simulate ongoing bleeding and air buildup. The image below shows the 5 products used and the animal setup:

Here are the factoids:

  • Creation of the open hemopneumothorax caused the intrapleural pressure to move toward atmospheric pressure as expected, resulting in labored breathing and reduced O2 saturation
  • Sealing the wound with any of the chest seal products corrected all of the problems just noted
  • Chest seals with one way valves did not evacuate blood efficiently (Bolin and SAM). The dressings either detached due to pooled blood, or the vent system clogged from blood clot.
  • Seals with laminar channels for drainage (see the pig picture above) allowed easy escape of blood and air
  • Success rates were 100% for Sentinel and Russell, 67% for HyFin, 25% for SAM, and 0% for Bolin

Bottom line: Prehospital providers need to be familiar with the products they use to cover open chest wounds. Totally occlusive dressings can result in development of a tension pneumothorax if there is an ongoing air leak from the lung. Vented chest seals are preferable for these injuries. Just be aware that vented seals with drainage channels perform much better than those that rely on a one-way valve.

Reference: Do vented chest seals differ in efficacy? An experimental
evaluation using a swine hemopneumothorax model. J Trauma 83(1):182-189, 2017.

The “Backward Finochietto” Problem

Resuscitative thoracotomy is a (sometimes) life-saving procedure reserved for trauma patients in extremis. Thankfully, most trauma centers do very few of these a year. However, that makes it one of those “high severity – low frequency” procedures that generate many, many quality improvement problems. Many of these issues are due to operator unfamiliarity or equipment availability.

Today, I’ll highlight a problem that crops up occasionally at various trauma centers across the US: the “backward Finochietto.” One of the most essential components of the resuscitative thoracotomy is rapid access to the chest. A large skin incision is typically made, the thoracic wall and intercostal musculature are divided, and the pleural space is entered.

It’s not easy to insinuate your arm between the ribs in an average person. But, of course, there’s a retractor for that! Von Mikulicz presented the first rib spreader at a German surgical society meeting in 1904.  Various versions of this instrument were devised over the next three decades to make it easier and faster to use.

The Finochietto retractor was introduced in 1936 and boasted several enhancements. It used a rack and pinion system to make it easier for the surgeon to spread the chest wall and made it unlikely to close on its own. The turning lever was hinged so it could flattened and placed out of the surgical field. The blades contained fenestrations so chest wall tissue could protrude into them and keep it from slipping when opened. It remains a workhorse instrument for us today and is found in most instrument packs for resuscitative thoracotomy.

But there is a potential problem. Some Finochietto retractors consist of only two pieces: a blade with the linear gear teeth (the rack) and another blade that fits onto it with the turning handle (the pinion). See the image below:

Looks great, right? However, there is one downside. The retractor parts that hook into the soft tissue are of a fixed depth. What if your patient has a more generous body habitus? Placing multiple sets of this retractor into the thoracotomy pack is not practical.

The solution is to allow detachable blades of various sizes. Here’s a modern-day example:

The good news is that the retractor tips are interchangeable. The bad news is that they are sometimes interchangeable with the wrong arm of the retractor! Hence the “backward Finochietto” problem. It’s impossible to use the retractors with the blades on the wrong side, and it takes time the trauma professional does not have to figure out how to snap them off and switch them around.

So what’s the solution? This is clearly an instrument reprocessing quality issue. These instruments are expensive, so your hospital may not be excited about purchasing new ones just for the trauma bay. It all boils down to foolproofing it in as many ways as possible.  Here are some tips:

  • Provide an educational session for all of the reprocessing techs. Unfortunately, this effect will wear off as staff turnover occurs.
  • Post a photograph of a properly assembled retractor for the techs to use when processing the tray.
  • Use colored instrument marking tape on each piece of the instrument. For example, a green tape strip should be placed on both the rack arm of the retractor and the left blade. Use red tape for the pinion arm and the right blade. All the tech needs to do now is match the colors as they assemble the retractor.

Bottom line: This problem is more common than you may think. Ask one of your old-timer trauma surgeons and I’ll bet they can tell you some stories. But it is easily avoided with a little creativity and some tape! Be sure to do it now so it doesn’t pop up in the heat of a resuscitative thoracotomy .

What You Need To Know About Blunt Cardiac Injury

Blunt cardiac injury can be an enigma. Significant injuries are uncommon, and the literature on it consists of case reports and small series. The group at Scripps La Jolla has an excellent review article on the topic that is currently in press. This post will relate some of the key points in this nicely prepared article.

  • Use the correct nomenclature. For years, many have called this condition “cardiac contusion” or “myocardial contusion.” Unfortunately, these descriptors are too specific. The proper term is “blunt cardiac injury (BCI),” which encompasses the entire gamut of injury from asymptomatic contusion to pericardial injury to cardiac rupture.
  • BCI occurs more commonly than you think. If one defines BCI as any arrhythmia or cardiac enzyme elevation, it is fairly common. However, if the definition is limited to clinically significant sequelae such as potentially malignant arrhythmia or cardiac failure, the incidence is easily less than 1% in blunt trauma patients.
  • Be aware of the usual mechanisms of injury. This is a condition caused by blunt trauma, with motor vehicle crashes causing half and pedestrians struck by them another one-third. Motorcycle crashes and falls caused the remaining 12%.
  • Diagnosis can be challenging.
    • Physical examination is usually of little help. New onset of a heart murmur may indicate a serious cardiac injury but is exceedingly rare.
    • EKG evidence of a new onset arrhythmia is important, particularly bundle branch blocks, PVCs, and ST segment / T wave changes, which require further investigation.
    • CPK-MB enzyme measurements are useless. Please don’t get them.
    • Troponin T and Troponin I are frequently used but do not reliably predict BCI. Testing in asymptomatic patients is not helpful and may result in additional asymptomatic testing.
    • Echocardiography is not indicated in asymptomatic patients with isolated enzyme elevations.
    • Cardiac CT may be used to differentiate acute MI from BCI. Frequently, patients at risk are having a chest CT with contrast performed anyway.

Here is the recommended treatment algorithm:

  1. If BCI is possible based on mechanism of injury, follow the ATLS protocols and perform a physical exam, E-FAST, and place on EKG monitoring.
  2. If the patient is hemodynamically unstable, quickly identify and treat tamponade or tension pneumothorax if present. If significant arrhythmias are present, treat with appropriate medications. If heart failure is present, treat medically and evaluate for surgical problems such as valve, septum, or coronary artery injury.
  3. If the patient is hemodynamically stable, obtain a 12 lead EKG. If significant arrythmias are present, treat with appropriate medications. If there is organ hypoperfusion, obtain an echocardiogram. If this study reveals an effusion, a pericardial window is indicated. If the echo shows hypokinesis or structural injury, appropriate medical or surgical management should be carried out.
  4. Patients who have only significant arrhythmias should be admitted to a monitored bed for 24 hours. Once arrhythmias have resolved, the patent can be discharged.
  5. Patients with nonspecific EKG changes should have troponin levels drawn after 8 hours of observation in the ED. If elevated, admit to a monitored bed for 24 hours. Once EKG and troponin have normalized, the patent can be discharged.
  6. If EKG and labs are normal, may discharge home from the ED if there are no other indications for admission.

Reference: Diagnosis and Management of Blunt Cardiac Injury: What You Need to Know. J Trauma, accepted for publication. DOI: 10.1097/TA.0000000000004216